Histidinemia

Alternative Names

  • Histidine Ammonia-Lyase Deficiency
  • HAL Deficiency
  • Histidase Deficiency
  • HIS Deficiency
Back to search Result
WHO-ICD-10 version:2010

Endocrine, nutritional and metabolic diseases

Metabolic disorders

OMIM Number

235800

Mode of Inheritance

Autosomal recessive

Gene Map Locus

12q23.1

Description

Histidinemia is a metabolic disorder characterized by increased levels of histidine in blood, urine, and cerebrospinal fluid, and decreased levels of the metabolite urocanic acid in blood, urine, and skin cells. Although histidinemia was originally associated with mental retardation and speech defects, it is generally considered to be a benign disorder. However, it is possible that histidinemia may be a risk factor for developmental disorders in certain individuals under specific circumstances, such as perinatal events. [From OMIM]

Epidemiology in the Arab World

View Map

Other Reports

Lebanon

In a retrospective analysis of IEMs diagnosed over a 12-year period (1998-2010) in a hospital in Lebanon, Karam et al. (2013) found one patient diagnosed with histidinemia. The patient was diagnosed at the age of 1 year and 3-months. 

© CAGS 2024. All rights reserved.